| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401722-67402117 | Common:3; Rare:140 | ||||
| chr11:67420779-67421011 | Common:2; Rare:56 | ||||
| chr11:67421084-67421452 | Common:5; Rare:125 | ||||
| chr11:67428098-67428594 | Common:1; Rare:153 | ||||
| chr11:67442810-67443018 | Common:2; Rare:38 | ||||
| chr11:67443390-67444015 | Common:3; Rare:174 | ||||
| chr11:67464608-67465003 | Rare:187 | ||||
| chr11:67465073-67465114 | Rare:10 | ||||
| chr11:67465190-67465526 | Rare:65 | ||||
| chr11:67468834-67469024 | Rare:57 | ||||
| chr11:67469132-67469488 | Common:4; Rare:122 | ||||
| chr11:67482824-67483199 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr11:67483222-67483579 | Common:1; Rare:109; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67505301-67505529 | Rare:58 | ||||
| chr11:67507820-67507952 | Rare:37 |